IS30969 AND nstd71 - dbVar - NCBI

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Items: 17

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv902149	copy number variation	1	nstd71	human		NCBI36 chr14: 82,728,476-82,815,943 , GRCh37.p13 chr14: 83,658,723-83,746,190 , GRCh38.p12 chr14: 83,192,379-83,279,846	LOC107984645
nsv871759	copy number variation	14	nstd71	human		NCBI36 chr1: 80,287,294-80,329,403 , GRCh37.p13 chr1: 80,514,706-80,556,815 , GRCh38.p12 chr1: 80,049,021-80,091,130	LOC553139
nsv894411	copy number variation	8	nstd71	human		NCBI36 chr9: 138,606,913-138,641,922 , GRCh37.p13 chr9: 139,487,092-139,522,101 , GRCh38.p12 chr9: 136,592,640-136,627,649	LINC01451
nsv884822	copy number variation	2547	nstd71	human		NCBI36 chr6: 32,560,168-32,593,470 , GRCh37.p13 chr6: 32,452,190-32,485,492 , GRCh38.p12 chr6: 32,484,413-32,517,715	HLA-DRB5
nsv884186	copy number variation	17	nstd71	human		NCBI36 chr6: 31,383,825-31,398,785 , GRCh37.p13 chr6\|NT_167249.1: 2,609,591-2,624,528 , GRCh37.p13 chr6: 31,275,846-31,290,806 , GRCh37.p13 chr6\|NT_167246.1: 2,622,673-2,631,393 , GRCh38.p12 chr6\|NT_167249.2: 2,610,293-2,625,230 , GRCh38.p12 chr6\|NT_167246.2: 2,617,053-2,625,775 , GRCh38.p12 chr6: 31,308,069-31,323,029	LOC112267902
nsv884735	copy number variation	6	nstd71	human		NCBI36 chr6: 32,450,515-32,457,689 , GRCh37.p13 chr6\|NT_167246.1: 3,685,366-3,692,540 , GRCh37.p13 chr6: 32,342,537-32,349,711 , GRCh38.p12 chr6: 32,374,760-32,381,934 , GRCh38.p12 chr6\|NT_167246.2: 3,679,746-3,686,920	TSBP1-AS1
nsv898924	copy number variation	2	nstd71	human		NCBI36 chr12: 25,248,947-25,290,239 , GRCh37.p13 chr12: 25,357,680-25,398,972 , GRCh38.p12 chr12: 25,204,746-25,246,038	ETFRF1, KRAS
nsv879310	copy number variation	1929	nstd71	human		NCBI36 chr4: 69,076,346-69,179,871 , GRCh37.p13 chr4: 69,393,751-69,497,276 , GRCh38.p12 chr4: 68,528,033-68,631,558	LOC100422402, LOC100132651, 2 more genes
nsv882084	copy number variation	25	nstd71	human		NCBI36 chr5: 70,232,726-70,300,876 , GRCh37.p13 chr5: 70,196,970-70,265,120 , GRCh38.p12 chr5: 70,901,143-70,969,293	SERF1A, NAIP, 2 more genes
nsv876827	copy number variation	19	nstd71	human		NCBI36 chr3: 57,426,028-57,483,578 , GRCh37.p13 chr3: 57,450,988-57,508,538 , GRCh38.p12 chr3: 57,465,261-57,522,811	RNF7P1, RNU6-1181P, 1 more genes
nsv881860	copy number variation	23	nstd71	human		NCBI36 chr5: 69,315,833-69,436,209 , GRCh37.p13 chr5: 69,280,077-69,400,453 , GRCh38.p12 chr5: 69,984,250-70,104,626 , GRCh38.p12 chr5\|NT_187651.1: 243,313-329,959	SMN2, CDH12P2, 6 more genes
nsv874770	copy number variation	1	nstd71	human		NCBI36 chr2: 107,904,055-108,476,458 , GRCh37.p13 chr2: 108,537,623-109,110,026 , GRCh38.p12 chr2: 107,921,167-108,493,570	SULT1C4, SETD6P1, 13 more genes
nsv882956	copy number variation	1	nstd71	human		NCBI36 chr5: 140,169,075-140,241,861 , GRCh37.p13 chr5\|NW_004775428.1: 44,482-117,268 , GRCh37.p13 chr5: 140,188,891-140,261,677 , GRCh38.p12 chr5: 140,809,306-140,882,092	PCDHA14, PCDHA12, 14 more genes
nsv894683	copy number variation	1	nstd71	human		NCBI36 chr9: 140,033,654-140,273,252 , GRCh37.p13 chr9: 140,913,833-141,153,431 , GRCh38.p12 chr9: 138,019,381-138,262,981	TUBBP5, FAM157B, 6 more genes
nsv908091	copy number variation	2	nstd71	human		NCBI36 chr17: 31,444,192-31,511,943 , GRCh37.p13 chr17\|NW_003315949.1: 1-45,210 , GRCh37.p13 chr17: 34,442,621-34,487,830 , GRCh38.p12 chr17\|NT_187661.1: 46,828-114,553 , GRCh38.p12 chr17\|NT_187614.1: 327,607-395,358 , GRCh38.p12 chr17: 36,092,731-36,160,457	LOC101927369, CCL4, 5 more genes
nsv889344	copy number variation	1	nstd71	human		NCBI36 chr7: 143,495,603-143,705,862 , GRCh37.p13 chr7: 143,864,670-144,074,929 , GRCh38.p12 chr7: 144,167,577-144,377,836	ARHGEF35-AS1, ARHGEF34P, 12 more genes
nsv901284	copy number variation	43	nstd71	human		NCBI36 chr14: 19,261,709-19,463,414 , GRCh37.p13 chr14: 20,191,869-20,393,574 , GRCh38.p12 chr14: 19,723,710-19,925,415	OR4N1P, LOC100421751, 11 more genes

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